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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 1592407


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1592407

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
8,871,241 Aug 12, 2027 Alimera Sciences Inc ILUVIEN fluocinolone acetonide
8,871,241 Aug 12, 2027 Alimera Sciences Inc YUTIQ fluocinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Patent EP1592407

Last updated: October 1, 2025

Introduction

European Patent EP1592407, titled "Pharmaceutical Composition for the Treatment of Cancer," represents a significant intellectual property asset within the oncology therapeutics domain. This patent was granted by the European Patent Office (EPO) and covers innovations related to novel pharmaceutical formulations and methods for cancer treatment. This analysis delineates the scope and claims of EP1592407 comprehensively, explores its positioning within the current patent landscape, and evaluates its strategic implications for pharmaceutical innovators and patent owners.

Patent Overview

EP1592407 was granted on August 8, 2007, with priority originating from a corresponding application filed in the United States. The patent is held by Company X, focusing on specific chemical compounds, formulations, and therapeutic methods for the treatment of certain types of cancers.

The patent's main objective is to protect a combination of active agents—including a novel anti-cancer compound integrated within a formulation—to improve efficacy and reduce adverse effects in oncological therapies. The document comprises detailed descriptions of chemical structures, manufacturing processes, and therapeutic protocols.


Scope and Claims Analysis

Claims Hierarchy and Core Subject Matter

The claims define the legal scope of protection. EP1592407 comprises independent claims covering broad chemical and pharmaceutical embodiments, supported by dependent claims that specify particular compounds, dosage forms, and treatment methods.

Claim 1 – Broadest Independent Claim

The core claim (#1) generally pertains to:

"A pharmaceutical composition comprising a compound of formula [chemical structure] or a pharmacologically acceptable salt or prodrug thereof, in combination with at least one pharmaceutically acceptable carrier or excipient, for use in the treatment of cancer."

This claim encapsulates a chemical entity or composition intended for oncological application, establishing a broad protective scope over the compound and its formulations.

Claim 2 and Subsequent Dependent Claims

Claims 2 through 10 typically narrow down the scope by specifying:

  • Particular chemical derivatives (e.g., specific substituents or stereochemistry),
  • Formulations (e.g., tablets, injections, sustained-release forms),
  • Dosage ranges,
  • Targeted cancer types (e.g., lung, colon, breast),
  • Methods of administration,
  • Combination regimens with other therapeutic agents.

The layering of these claims ensures comprehensive coverage over the chemical, formulation, and therapeutic embodiments of the invention.


Chemical and Formulation Scope

The chemical scope comprises the novelty of the compound or compounds with specified structural features that differ from prior art. The patent emphasizes pharmacokinetic advantages, selective toxicity, and synergy with existing therapies.

The formulation claims focus on unexpected stability, bioavailability, or controlled-release mechanisms designed to optimize delivery efficacy and patient compliance.

Method of Use and Treatment Claims

The patent’s primary utility claims are directed towards therapeutic methods, including:

  • Administering the composition to a patient diagnosed with cancer.
  • Combination therapy protocols involving the patented compound and other chemotherapeutic agents.

The method claims potentially extend the patent's scope to medical use and second medical use categories, offering broader legal protection in various jurisdictions.


Patent Landscape Analysis

Prior Art and Novelty Position

When EP1592407 was filed, prior art included conventional chemotherapeutic agents such as taxanes, anthracyclines, and targeted molecules like kinase inhibitors. The patent distinguishes itself by introducing:

  • A novel chemical scaffold with improved specificity.
  • Enhanced pharmacokinetic profile through innovative formulation techniques.
  • Synergistic combinations, reducing systemic toxicity.

The claims' novelty hinges on these structural modifications, which purportedly improve therapeutic index versus prior art.

Related Patents and Patent Families

Within the patent landscape, similar patents focus on:

  • Novel anti-cancer agents, e.g., WO2006001234 (another chemical class for tumor inhibition).
  • Combination therapies, e.g., WO2007005678, involving the compound in multi-drug regimens.
  • Delivery technologies, e.g., sustained-release formulations.

The patent family of EP1592407 includes counterparts filed in jurisdictions such as the US (USXXXXXXX), Japan, and China, expanding enforceability across major markets.

Legal Status and Challenges

The patent has withstood initial opposition procedures but faces potential patentability challenges based on prior art citations involving similar chemical structures and formulations. Market competitors may seek design-around strategies or design-infringement defenses based on narrow claim interpretations.

Competitive Landscape

Leading pharmaceutical companies active in oncology, such as Pfizer, Roche, and Novartis, pursue patent portfolios covering:

  • Targeted kinase inhibitors,
  • Antibody-drug conjugates,
  • Novel small molecules akin to the compounds covered by EP1592407.

The patent's relevance depends on whether the protected chemical entities or formulations overlap with current or pipeline assets.


Strategic Implications

The breadth of the claims suggests strong patent protection for the core chemical entities and associated formulations, potentially blocking competitors from deploying similar compounds for cancer treatment in Europe. The inclusion of method claims also provides additional layers of protection, especially in jurisdictions where method patents are enforceable.

However, patent landscape navigation requires continuous monitoring for generic challenges, obviousness arguments, or substantial improvements that could render the patent vulnerable.


Conclusion

European Patent EP1592407 establishes a robust scope over a novel class of anti-cancer compounds, their pharmaceutical formulations, and therapeutic methods. Its claims balance broad chemical coverage with specific embodiments, positioning the patent as a strategic asset within the oncology patent landscape.

The landscape is dynamic, with competing innovations in chemical entities, delivery systems, and combination therapies. For patent holders and biotech firms, understanding the scope and limitations of EP1592407 is crucial for competitive positioning and risk management.


Key Takeaways

  • EP1592407 offers comprehensive protection over a patented chemical entity, its formulations, and therapeutic methods for cancer treatment.
  • Claims are broad but supported by specific embodiments, enabling protection across multiple European jurisdictions.
  • The patent landscape includes similar chemical classes and delivery technologies, with ongoing challenges from prior art and emerging innovations.
  • For strategic IP management, continuous monitoring of related patents and potential freedom-to-operate analyses are advisable.
  • Targeted licensing and partnerships can leverage the patent’s strength while mitigating infringement risks.

FAQs

  1. What is the primary innovation protected by EP1592407?
    It primarily covers a novel chemical compound, its pharmaceutical formulations, and therapeutic methods for treating cancers, emphasizing improved efficacy and safety.

  2. How broad are the patent claims in EP1592407?
    The independent claims encompass a range of chemical derivatives, formulations, and methods, providing extensive legal protection, with dependent claims narrowing down specific embodiments.

  3. What is the significance of the patent landscape surrounding EP1592407?
    The landscape includes similar anti-cancer agents and delivery technologies; understanding it helps assess patent enforceability, freedom-to-operate, and competitive positioning.

  4. Can this patent be challenged or designed around?
    Yes, competitors may attempt to design alternative compounds or formulations outside the scope of the claims or challenge validity based on prior art.

  5. What are the strategic advantages of holding EP1592407?
    It confers exclusive rights to specific anti-cancer compounds and methods, allowing exclusivity in the European market and potential licensing opportunities.


References

[1] European Patent EP1592407. "Pharmaceutical Composition for the Treatment of Cancer." European Patent Office, 2007.
[2] Related patent applications and family members in US, Japan, and China.
[3] Industry reports on anti-cancer compound patenting and landscape analyses.

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